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[1,1'-Bicyclohexyl]-1,1'-dicarboxylic acid, dimethyl ester is a chemical compound with the molecular formula C20H28O4. It is a dimethyl ester derivative of 1,1'-bicyclohexyl-4,4'-dicarboxylic acid and is characterized by its white solid appearance, high melting point, and low solubility in water. [1,1'-Bicyclohexyl]-1,1'-dicarboxylic acid, dimethyl ester is known for its versatile nature and synthesis pathways, making it a promising candidate for various applications across different industries.

4368-59-6

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4368-59-6 Usage

Uses

Used in Chemical Synthesis:
[1,1'-Bicyclohexyl]-1,1'-dicarboxylic acid, dimethyl ester is used as an intermediate in the synthesis of specialty chemicals and polymers. Its unique chemical structure and properties contribute to the development of new materials with specific characteristics, enhancing the performance and functionality of the end products.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, [1,1'-Bicyclohexyl]-1,1'-dicarboxylic acid, dimethyl ester is used as a key component in the development of new drugs. Its unique chemical structure allows for the creation of novel molecules with potential therapeutic effects, addressing various medical conditions and improving patient outcomes.
Used in Agrochemical Applications:
[1,1'-Bicyclohexyl]-1,1'-dicarboxylic acid, dimethyl ester is also utilized in the agrochemical sector, where it serves as a building block for the development of new pesticides and other agricultural chemicals. Its incorporation into these products can lead to improved efficacy, reduced environmental impact, and enhanced safety for both humans and the ecosystem.
Used in Materials Science:
In the field of materials science, [1,1'-Bicyclohexyl]-1,1'-dicarboxylic acid, dimethyl ester is used as a component in the development of advanced materials with specific properties. These materials can be employed in various applications, such as electronics, automotive, aerospace, and construction industries, where their unique characteristics can provide significant advantages.
Used in Technology Development:
[1,1'-Bicyclohexyl]-1,1'-dicarboxylic acid, dimethyl ester may also have potential uses in the development of new technologies and materials due to its versatile nature and synthesis pathways. Its incorporation into innovative products can lead to the creation of cutting-edge solutions that address current challenges and drive progress in various sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 4368-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4368-59:
(6*4)+(5*3)+(4*6)+(3*8)+(2*5)+(1*9)=106
106 % 10 = 6
So 4368-59-6 is a valid CAS Registry Number.

4368-59-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-(1-methoxycarbonylcyclohexyl)cyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names Dimethyl-bicyclohexyl-1,1'-dicarboxylat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4368-59-6 SDS

4368-59-6Downstream Products

4368-59-6Relevant academic research and scientific papers

COUPLING REACTIONS OF VINYLKETENE SILYL ACETALS PROMOTED BY TITANIUM TETRACHLORIDE

Hirai, Kenji,Ojima, Iwao

, p. 785 - 788 (2007/10/02)

Homo- and cross-couplings of vinylketene silyl acetals were found to be effectively promoted by titanium tetrachloride to give the corresponding unsaturated diesters in good yields.The reactions between two different ketene silyl acetals afforded the corresponding cross-coupling products in unexpectedly good selectivities.

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